Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Andrzej Roszkiewicz"'
Publikováno v:
Polish journal of pathology : official journal of the Polish Society of Pathologists. 66(2)
Publikováno v:
European Journal of Pediatric Surgery. 9:343-346
Un cas de pseudotumeur hepatique de type inflammatoire simulant la malignite est rapporte chez une fille de 4 ans atteinte du syndrome de Papillon-Lefevre (PLS). C'est seulement recemment qu'on a decouvert une association entre ce syndrome hereditair
Autor:
Janusz Rys, Andrzej Roszkiewicz, Markku Miettinen, Krzysztof Mrózek, Niezabitowski A, Maria Debiec-Rychter, Zenon Gibas, Bogusław Nedoszytko, Janusz Limon
Publikováno v:
American Journal of Clinical Pathology. 103:20-26
Cytogenetic and immunohistochemical studies were performed in nine myxoid liposarcomas. The tumor karyotype was determined after short-term culture of cells in vitro. Immunohistochemical studies were performed on frozen tissue in five cases and on pa
Autor:
Czes≥aw Stoba, Mariola Iliszko, Piotr Czauderna, Ma≥gorzata BabiÒska, Janusz Limon, Andrzej Roszkiewicz
Publikováno v:
Cancer Genetics and Cytogenetics. 102:142-144
An undifferentiated embryonal sarcoma (malignant mesenchymoma) of the liver from a 5-year-old girl was found to have near-triploid and near-hexaploid clones with several chromosomal rearrangements. This is the first description of the chromosomal cha
Autor:
Małgorzata Babińska, Piotr Hadaczek, Iwona Kardas, Krzysztof Mrózek, Janusz Limon, Kazimierz Krajka, Ewa Kuziemska, Jan Lubinski, Andrzej Roszkiewicz
Publikováno v:
Oncology reports. 13(5)
Cytogenetic analysis of 75 clear cell renal cell carcinomas (RCC) from adult patients revealed abnormal karyotypes in 59 (79%) tumors. Among structural abnormalities, the most frequent were deletions and unbalanced translocations leading to loss of 3
Autor:
Krzysztof Mrózek, Maciej Świerblewski, Bogusław Nedoszytko, Andrzej Roszkiewicz, Janusz Limon, Andrzej Kopacz
Publikováno v:
Cancer Genetics and Cytogenetics. 91:37-39
Cytogenetic analysis performed on a specimen from an inguinal lymph node metastasis of a tumor diagnosed initially as a cutaneous malignant melanoma revealed the following karyotype: 50, XX, +2, +7, +8, +8, t(12;22) (q13;q12). The finding of t(12;22)
Autor:
Maria Debiec-Rychter, Andrzej Kopacz, Janusz Jaśkiewicz, Małgorzata Babińska, Janusz Limon, Anna Szadowska, Andrzej Roszkiewicz, K. Mrózek, Mariola Iliszko
Publikováno v:
Genes, chromosomescancer. 21(2)
Cytogenetic analysis of two adult fibrosarcomas revealed clonal chromosomal rearrangements including unbalanced translocations between chromosomes 2 and 19, with the same segment, 2q21-qter, translocated onto 19p13 in one tumor and 19q13 in another;
Publikováno v:
Biochemical and Biophysical Research Communications. 86:801-807
When rat liver mitochondria were exposed to protamine or butylmalonate, succinate oxidation was inhibited. However, butylmalonate was found to release the inhibitory effect of protamine on succinate oxidation in mitochondria. Electron microscopic stu
Autor:
Marianna Soroka, Andrzej Bernaczyk, Ewa Matyja, Anna Jakubowska, Cezary Cybulski, Grażyna Bierzyńska-Macyszyn, Andrzej Roszkiewicz, Bogdan Woźniewicz, Tadeusz Dębniak, Jan Lubinski, Alicja Markowska-Wojciechowska, Radzisław Kordek, Edmund Prudlak, Bohdan Górski, Krzysztof Zieliński, Lech Zimnoch, Tomasz Trojanowski, Wojciech Kozłowski, Anna Taraszewska, Teresa Wierzba-Bobrowicz, Tadeusz Szylberg, Przemysław Nowacki, Janusz Szymaś, Joanna Matyjasik
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 2, Iss 2, Pp 93-97 (2004)
Hereditary Cancer in Clinical Practice
Hereditary Cancer in Clinical Practice
Central nervous system hemangioblastomas (cHAB) are rare tumours which most commonly arise in the cerebellum. Most tumours are sporadic, but as many as one third of cHABs occur in the course of the hereditary disorder - von Hippel-Lindau disease (VHL